Chao Chi-Chao, Hsieh Sung-Tsang, Shun Chia-Tung, Hsieh Song-Chou
Department of Neurology, National Taiwan University Hospital, 7 Chung-Shan S Rd, Taipei 10002, Taiwan.
Arch Neurol. 2007 Jul;64(7):959-65. doi: 10.1001/archneur.64.7.959.
Eosinophilia is frequently associated with peripheral neuropathy, and neuropathic pain is a major presentation. Little is known about the involvement of sensory nerve terminals and the vasculature in the skin of patients with eosinophilia.
To investigate the skin innervation and the pathological abnormalities of the cutaneous vasculature and their clinical significance in eosinophilia-associated neuropathy.
Case series.
National Taiwan University Hospital, Taipei, Taiwan. Patients Twelve patients with neuropathy and concomitant eosinophilia (with an eosinophilic ratio of white blood cell classification > 10% or absolute eosinophil count of > 1000/microL).
Clinical assessments of neurological deficits, laboratory tests, nerve conduction studies, and a skin biopsy specimen 3 mm in diameter taken from the distal leg without active skin lesions.
Quantitation of epidermal innervation, immunopathological findings of the cutaneous vasculature, and motor disability grade.
Six patients fulfilled the criteria of Churg-Strauss syndrome, and the other 6 patients were categorized as having primary eosinophilia. All of the 12 patients had mononeuropathy multiplex or polyneuropathy with sensory symptoms as the initial manifestation. Intraepidermal nerve fiber densities were reduced in 10 patients (83.3%), being significantly lower than in the controls (mean +/- SD, 2.12 +/- 2.30 vs 10.56 +/- 3.69 fibers/mm, respectively; P < .001) and negatively correlated with the disability grade (P = .003). Nine patients (75.0%), including all of the 6 patients with Churg-Strauss syndrome, had cutaneous vasculitis, and two-thirds of the 9 patients had perivascular infiltration of eosinophils.
Skin denervation with cutaneous vasculitis is a major manifestation of eosinophilia-associated neuropathy.
嗜酸性粒细胞增多常与周围神经病变相关,神经病理性疼痛是主要表现。关于嗜酸性粒细胞增多患者皮肤中感觉神经末梢和脉管系统的情况知之甚少。
研究嗜酸性粒细胞增多相关神经病变中皮肤神经支配、皮肤脉管系统的病理异常及其临床意义。
病例系列研究。
台湾台北国立台湾大学医院。患者12例伴有神经病变和嗜酸性粒细胞增多的患者(白细胞分类中嗜酸性粒细胞比例>10%或绝对嗜酸性粒细胞计数>1000/微升)。
进行神经功能缺损的临床评估、实验室检查、神经传导研究,并从无活动性皮肤病变的小腿远端取直径3毫米的皮肤活检标本。
表皮神经支配的定量分析、皮肤脉管系统的免疫病理结果以及运动功能障碍分级。
6例患者符合Churg-Strauss综合征标准,另外6例患者归类为原发性嗜酸性粒细胞增多。12例患者均以多发性单神经病或多发性神经病伴感觉症状为首发表现。10例患者(83.3%)表皮内神经纤维密度降低,显著低于对照组(分别为平均±标准差,2.12±2.30与10.56±3.69条纤维/毫米;P<.001),且与功能障碍分级呈负相关(P=.003)。9例患者(75.0%),包括所有6例Churg-Strauss综合征患者,有皮肤血管炎,9例患者中有三分之二有嗜酸性粒细胞血管周围浸润。
皮肤去神经支配伴皮肤血管炎是嗜酸性粒细胞增多相关神经病变的主要表现。